Canonical Allele Identifier: CA2238191783

Gene: HSBP1 CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83745223_83745264delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT , CM000678.2:g.83745223_83745264delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT	GRCh38
NC_000016.9:g.83778828_83778869delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT , CM000678.1:g.83778828_83778869delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT	GRCh37
NC_000016.8:g.82336329_82336370delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT	NCBI36
NG_052819.1:g.1123430_1123471delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000690173.1:n.97+25816_97+25857delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (HSBP1)
ENST00000693379.1:n.97+25816_97+25857delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (HSBP1)
ENST00000693758.1:n.97+25816_97+25857delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (HSBP1)
ENST00000567109.6:c.1539-2885_1539-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13) MANE Select	ENSP00000479395.1:n.1539-2885_1539-2844delinsAGGCCAGACGCCTTCC...
ENST00000268613.14:c.1680-2885_1680-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000268613.10:n.1680-2885_1680-2844delinsAGGCCAGACGCCTTC...
ENST00000428848.7:c.1422-2885_1422-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000394557.3:n.1422-2885_1422-2844delinsAGGCCAGACGCCTTCC...
ENST00000539548.6:c.*1171-2885_*1171-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000442225.2:n.*1171-2885_*1171-2844delinsAGGCCAGACGCCTT...
ENST00000566620.5:c.1503-2885_1503-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000454435.3:n.1503-2885_1503-2844delinsAGGCCAGACGCCTTCC...
ENST00000567109.5:c.1539-2885_1539-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000479395.1:n.1539-2885_1539-2844delinsAGGCCAGACGCCTTCC...
ENST00000615627.1:c.459-2885_459-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000482651.1:n.459-2885_459-2844delinsAGGCCAGACGCCTTCCAG...
ENST00000622885.4:c.1383-2885_1383-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	ENSP00000483719.1:n.1383-2885_1383-2844delinsAGGCCAGACGCCTTCC...
NM_001220488.1:c.1680-2885_1680-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001207417.1:n.1680-2885_1680-2844delinsAGGCCAGACGCCTTCCAGG...
NM_001220489.1:c.1422-2885_1422-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001207418.1:n.1422-2885_1422-2844delinsAGGCCAGACGCCTTCCAGG...
NM_001220490.1:c.777-2885_777-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001207419.1:n.777-2885_777-2844delinsAGGCCAGACGCCTTCCAGGAA...
NM_001257.4:c.1539-2885_1539-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001248.1:n.1539-2885_1539-2844delinsAGGCCAGACGCCTTCCAGGAAG...
XM_011522804.1:c.1236-2885_1236-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	XP_011521106.1:n.1236-2885_1236-2844delinsAGGCCAGACGCCTTCCAGG...
XM_011522804.3:c.1236-2885_1236-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	XP_011521106.1:n.1236-2885_1236-2844delinsAGGCCAGACGCCTTCCAGG...
NM_001257.5:c.1539-2885_1539-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13) MANE Select	NP_001248.1:n.1539-2885_1539-2844delinsAGGCCAGACGCCTTCCAGGAAG...
NM_001220488.2:c.1680-2885_1680-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001207417.1:n.1680-2885_1680-2844delinsAGGCCAGACGCCTTCCAGG...
NM_001220489.2:c.1422-2885_1422-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001207418.1:n.1422-2885_1422-2844delinsAGGCCAGACGCCTTCCAGG...
NM_001220490.2:c.777-2885_777-2844delinsAGGCCAGACGCCTTCCAGGAAGCATCAGCAGGAGCCTCTCCT (CDH13)	NP_001207419.1:n.777-2885_777-2844delinsAGGCCAGACGCCTTCCAGGAA...